80371-90-0

Basic information

• Product Name: 3-[(2-hydroxyethyl)amino]-5,5-dimethylcyclohex-2-ene-1-thione
• CAS NO: 80371-90-0
• Molecular Weight: 199.317
• Mol File: 80371-90-0.mol

Chemical Properties

• CAS DataBase Reference: 3-[(2-hydroxyethyl)amino]-5,5-dimethylcyclohex-2-ene-1-thione(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[(2-hydroxyethyl)amino]-5,5-dimethylcyclohex-2-ene-1-thione(80371-90-0)
• EPA Substance Registry System: 3-[(2-hydroxyethyl)amino]-5,5-dimethylcyclohex-2-ene-1-thione(80371-90-0)

Safety Data

• Hazardous Substances Data: 80371-90-0(Hazardous Substances Data)

Upstream product

• 141-43-5 ethanolamine 
• 267899-74-1 bis(5,5-dimethyl-3-thioxocyclohex-1-en-1-yl) sulfide 
• 70134-11-1 N-(5,5-Dimethyl-3-methoxy-cyclohex-2-en-1-yliden)-morpholinium 
• 80371-87-5 N-(3-methoxy-5,5-dimethyl-2-cyclohexen-1-ylidene)pyrrolidinium iodide 
• 70134-09-7 3-Methoxy-5,5-dimethyl-2-cyclohexene-1-thione 

Relevant articles and documents

1,7-dithioxo systems. Reaction of 3-[(5,5-dimethyl-3-thioxocyclohex-1-en-1yl)sulfanyl]-5,5-dimethylcyclohex-2-ene-1-thione with 2-aminoethanol and ethane-1,2-diamine

The reaction of 3-[(5,5-dimethyl-3-thioxocyclohex-1-en-1-yl)sulfanyl]-5,5-dimethylcyclohex-2-ene-1-thione with 2-aminoethanol involves cleavage of the sulfide bond with formation of 3-[(2-hydroxyethyl)-amino]-5,5-dimethylcyclohex-2-ene-1-thione as the maj

α,β-UNSATURATED THIO COMPOUNDS. XIII.* HYDROTHIOLYSIS OF β-HETERO-SUBSTITUTED α,β-UNSATURATED IMMONIUM SALTS AT THE C=N(+) BOND - A GENERAL APPROACH TO THE SYNTHESIS OF FUNCTIONALLY SUBSTITUTED THIOKETONES

The hydrothiolysis of immonium salts containing the Y-C=C-C=N(+) group takes place at the C=N(+) bond and not at the C-Y bond.This is consistent with the results from quantum-chemical calculations.On this basis a general approach was formulated to the synthesis of new types of organic sulfur compounds, i.e. β-alkoxy-, β-alkylthio-, and β-halogen-substituted α,β-unsaturated thioketones of the Y-C=C-C=S (Y=RO, RS, Hlg) type.